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雄性大鼠脊髓损伤对生殖系细菌感染及IL-1、TNF-α、SOD表达的影响 被引量:1

Spinal cord injury in male rats can impact bacterial infection of reproductive system,and IL-1,TNF-α and SOD expressions
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摘要 目的:了解脊髓损伤后雄性大鼠前列腺、附睾、睾丸细菌感染及IL-1、TNF-α、SOD蛋白的表达情况。方法:80只SD大鼠采用随机数字法分为对照组(n=40)和实验组(n=40),采用改良Allen法建立脊髓损伤动物模型,分别喂养1、2、4、8、16 d,2组均于每个时间点摘取8只大鼠的前列腺、附睾、睾丸组织进行细菌培养和免疫组织化学SABC法检测白介素-1(Interleukin-1,IL-1)、肿瘤坏死因子-α(Tumor necrosis factor-α,TNF-α)、超氧化物歧化酶(Superoxide dismutase,SOD)的表达。结果:与对照组相比,实验组前列腺、附睾细菌培养阳性数显著提高(P<0.05),大肠杆菌的检出率高于其他细菌;睾丸IL-1、TNF-α表达明显增多(P<0.05),实验组间以术后第4天表达水平最高(P<0.05);SOD表达无明显差异(P>0.05)。结论:脊髓损伤后大鼠前列腺、附睾易受到以大肠杆菌为主的细菌感染,睾丸炎性反应增强,生殖系抗氧化反应可能很弱。 Objective:To study the expressions of IL-1,TNF-α,SOD and bacterial infection in male rats' reproductive system after spinal cord injury.Methods:80 SD rats were divided into control group(40 rats) and experimental group(40 rats) randomly.Animal models of spinal cord injury were established by 'Allen' method.Both groups of rats were fed for 1 day,2 days,4 days,8 days,and 16 days respectively.Then 8 rats' prostates,testes and epididymises in each group were extirpated for bacterial culture and immunohistochemistry by SABC to detect the expressions of proteins(IL-1,TNF-α,SOD) at each time point.Results:Compared with control group,the risk of E.coli infection in prostate and epididymis was increased significantly in the experimental group(P0.05);the expressions of testicular IL-1 and TNF-α were increased(P0.05) and the expression level was the highest in the fourth days after surgery(P0.05).SOD expression showed no significant difference in the whole reproductive system(P0.05).Conclusion:Prostate and epididymis of the rat after spinal cord injury are easily infected by bacteria(E.coli);inflammatory response was enhanced in testicular,and the antioxidant activity of reproductive system may be very weak.
出处 《重庆医科大学学报》 CAS CSCD 北大核心 2011年第11期1296-1299,共4页 Journal of Chongqing Medical University
基金 重庆市卫生局医学科研资助项目(编号:06-2-019)
关键词 脊髓损伤 生殖系 超氧化物歧化酶 白介素-1 肿瘤坏死因子-Α spinal cord injury reproductive system superoxide dismutase(SOD) interleukin-1(IL-1) tumor necrosis factor-α(TNF-α)
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